Issue 2, 2022

Catalyst-free visible light-induced decarboxylative amination of glycine derivatives with azo compounds

Abstract

α-Amino acids such as glycine derivatives have been utilized commonly as reagents for decarboxylative functionalization. In contrast to reports revealing the requirement of transition metals and organic dyes to promote this process, we report a catalyst-free approach for the decarboxylative amination of glycine derivatives with azo compounds under visible-light irradiation. A range of important aminals was obtained with high efficiency under mild reaction conditions.

Graphical abstract: Catalyst-free visible light-induced decarboxylative amination of glycine derivatives with azo compounds

Supplementary files

Article information

Article type
Communication
Submitted
26 Oct 2021
Accepted
16 Nov 2021
First published
30 Nov 2021

New J. Chem., 2022,46, 465-469

Catalyst-free visible light-induced decarboxylative amination of glycine derivatives with azo compounds

C. Zhou, X. Huang, Y. Hu, J. Wu, Y. Zheng and X. Zhang, New J. Chem., 2022, 46, 465 DOI: 10.1039/D1NJ05079F

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